A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741826



Internal ID20517804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87022534..87022595hg38UCSC Ensembl
chr4:87943686..87943747hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280341
Samples
Known GenesAFF1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741826
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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